United States · FDA National Drug Code directory

eteplirsen

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
61434-035_3c418de9-a70c-5616-e063-6394a90a1f22
Product NDC
61434-035
Form
INJECTION
Composition / generic term
eteplirsen
Labeler
Catalent Indiana, LLC
Marketing category
DRUG FOR FURTHER PROCESSING
Marketing start / end (source format)
20160919
Source listing expiry
20261231

Source-listed ingredients

  • ETEPLIRSEN — 500 mg/10mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 288 VIAL in 1 CASE (61434-035-01) / 10 mL in 1 VIAL · 61434-035-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →
eteplirsen — United States | Molindra Medicines